Canonical Allele Identifier: CA2452910314

Gene: HTR2C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.114903581C= , CM000685.2:g.114903581C=	GRCh38
NC_000023.10:g.114138144C= , CM000685.1:g.114138144C=	GRCh37
NC_000023.9:g.114044400C=	NCBI36
NG_012082.2:g.324497C=
NG_012082.3:g.324497C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000276198.6:c.551-3008C= MANE Select	ENSP00000276198.1:n.551-3008C=
ENST00000276198.5:c.551-3008C=	ENSP00000276198.1:n.551-3008C=
ENST00000371950.3:c.456-3008C=	ENSP00000361018.3:n.456-3008C=
ENST00000371951.5:c.551-3008C=	ENSP00000361019.1:n.551-3008C=
NM_000868.3:c.551-3008C=	NP_000859.1:n.551-3008C=
NM_001256760.2:c.551-3008C=	NP_001243689.1:n.551-3008C=
NM_001256761.2:c.456-3008C=	NP_001243690.1:n.456-3008C=
NM_000868.4:c.551-3008C= MANE Select	NP_000859.2:n.551-3008C=
NM_001256760.3:c.551-3008C=	NP_001243689.2:n.551-3008C=
NM_001256761.3:c.456-3008C=	NP_001243690.2:n.456-3008C=